-
1
-
-
13944268723
-
The RAD51 gene family, genetic instability and cancer
-
Thacker J. The RAD51 gene family, genetic instability and cancer. Cancer Lett. 219 (2005) 125-135
-
(2005)
Cancer Lett.
, vol.219
, pp. 125-135
-
-
Thacker, J.1
-
2
-
-
0037364415
-
RecQ helicases: caretakers of the genome
-
Hickson I.D. RecQ helicases: caretakers of the genome. Nat. Rev. Cancer 3 (2003) 169-178
-
(2003)
Nat. Rev. Cancer
, vol.3
, pp. 169-178
-
-
Hickson, I.D.1
-
3
-
-
0016336696
-
Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement
-
Schroeder T.M., and German J. Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement. Humangenetik 25 (1974) 299-306
-
(1974)
Humangenetik
, vol.25
, pp. 299-306
-
-
Schroeder, T.M.1
German, J.2
-
4
-
-
0030686496
-
The Bloom's syndrome gene product is a 3′-5′ DNA helicase
-
Karow J.K., Chakraverty R.K., and Hickson I.D. The Bloom's syndrome gene product is a 3′-5′ DNA helicase. J. Biol. Chem. 272 (1997) 30611-30614
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 30611-30614
-
-
Karow, J.K.1
Chakraverty, R.K.2
Hickson, I.D.3
-
5
-
-
0032939991
-
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
-
Kitao S., Shimamoto A., Goto M., Miller R.W., Smithson W.A., Lindor N.M., and Furuichi Y. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nat. Genet. 22 (1999) 82-84
-
(1999)
Nat. Genet.
, vol.22
, pp. 82-84
-
-
Kitao, S.1
Shimamoto, A.2
Goto, M.3
Miller, R.W.4
Smithson, W.A.5
Lindor, N.M.6
Furuichi, Y.7
-
6
-
-
0038288850
-
Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome
-
Wang L.L., Gannavarapu A., Kozinetz C.A., Levy M.L., Lewis R.A., Chintagumpala M.M., Ruiz-Maldanado R., Contreras-Ruiz J., Cunniff C., Erickson R.P., Lev D., Rogers M., Zackai E.H., and Plon S.E. Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome. J. Natl. Cancer Inst. 95 (2003) 669-674
-
(2003)
J. Natl. Cancer Inst.
, vol.95
, pp. 669-674
-
-
Wang, L.L.1
Gannavarapu, A.2
Kozinetz, C.A.3
Levy, M.L.4
Lewis, R.A.5
Chintagumpala, M.M.6
Ruiz-Maldanado, R.7
Contreras-Ruiz, J.8
Cunniff, C.9
Erickson, R.P.10
Lev, D.11
Rogers, M.12
Zackai, E.H.13
Plon, S.E.14
-
7
-
-
0034737004
-
Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome
-
Lindor N.M., Furuichi Y., Kitao S., Shimamoto A., Arndt C., and Jalal S. Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome. Am. J. Med. Genet. 90 (2000) 223-228
-
(2000)
Am. J. Med. Genet.
, vol.90
, pp. 223-228
-
-
Lindor, N.M.1
Furuichi, Y.2
Kitao, S.3
Shimamoto, A.4
Arndt, C.5
Jalal, S.6
-
8
-
-
20144383378
-
Tumor suppressor p53 represses transcription of RECQ4 helicase
-
Sengupta S., Shimamoto A., Koshiji M., Pedeux R., Rusin M., Spillare E.A., Shen J.C., Huang L.E., Lindor N.M., Furuichi Y., and Harris C.C. Tumor suppressor p53 represses transcription of RECQ4 helicase. Oncogene (2005)
-
(2005)
Oncogene
-
-
Sengupta, S.1
Shimamoto, A.2
Koshiji, M.3
Pedeux, R.4
Rusin, M.5
Spillare, E.A.6
Shen, J.C.7
Huang, L.E.8
Lindor, N.M.9
Furuichi, Y.10
Harris, C.C.11
-
9
-
-
15544389502
-
Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome
-
Mann M.B., Hodges C.A., Barnes E., Vogel H., Hassold T.J., and Luo G. Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome. Hum. Mol. Genet. (2005)
-
(2005)
Hum. Mol. Genet.
-
-
Mann, M.B.1
Hodges, C.A.2
Barnes, E.3
Vogel, H.4
Hassold, T.J.5
Luo, G.6
-
10
-
-
0034726966
-
Differential regulation of human RecQ family helicases in cell transformation and cell cycle
-
Kawabe T., Tsuyama N., Kitao S., Nishikawa K., Shimamoto A., Shiratori M., Matsumoto T., Anno K., Sato T., Mitsui Y., Seki M., Enomoto T., Goto M., Ellis N.A., Ide T., Furuichi Y., and Sugimoto M. Differential regulation of human RecQ family helicases in cell transformation and cell cycle. Oncogene 19 (2000) 4764-4772
-
(2000)
Oncogene
, vol.19
, pp. 4764-4772
-
-
Kawabe, T.1
Tsuyama, N.2
Kitao, S.3
Nishikawa, K.4
Shimamoto, A.5
Shiratori, M.6
Matsumoto, T.7
Anno, K.8
Sato, T.9
Mitsui, Y.10
Seki, M.11
Enomoto, T.12
Goto, M.13
Ellis, N.A.14
Ide, T.15
Furuichi, Y.16
Sugimoto, M.17
-
11
-
-
27144460601
-
The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability
-
Petkovic M., Dietschy T., Freire R., Jiao R., and Stagljar I. The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability. J. Cell Sci. 118 (2005) 4261-4269
-
(2005)
J. Cell Sci.
, vol.118
, pp. 4261-4269
-
-
Petkovic, M.1
Dietschy, T.2
Freire, R.3
Jiao, R.4
Stagljar, I.5
-
12
-
-
20444380748
-
Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome
-
Sangrithi M.N., Bernal J.A., Madine M., Philpott A., Lee J., Dunphy W.G., and Venkitaraman A.R. Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome. Cell 121 (2005) 887-898
-
(2005)
Cell
, vol.121
, pp. 887-898
-
-
Sangrithi, M.N.1
Bernal, J.A.2
Madine, M.3
Philpott, A.4
Lee, J.5
Dunphy, W.G.6
Venkitaraman, A.R.7
-
13
-
-
33646048761
-
Recql4 haploinsufficiency in mice leads to defects in osteoblast progenitors: implications for low bone mass phenotype
-
Yang J., Murthy S.M., Winata T., Werner S., Abe M., Prahalad A.K., and Hock J.M. Recql4 haploinsufficiency in mice leads to defects in osteoblast progenitors: implications for low bone mass phenotype. Biochem. Biophys Res. Commun. 344 (2006) 346-352
-
(2006)
Biochem. Biophys Res. Commun.
, vol.344
, pp. 346-352
-
-
Yang, J.1
Murthy, S.M.2
Winata, T.3
Werner, S.4
Abe, M.5
Prahalad, A.K.6
Hock, J.M.7
-
14
-
-
0019843761
-
Hydrogen peroxide and human cataract
-
Spector A., and Garner W.H. Hydrogen peroxide and human cataract. Exp. Eye Res. 33 (1981) 673-681
-
(1981)
Exp. Eye Res.
, vol.33
, pp. 673-681
-
-
Spector, A.1
Garner, W.H.2
-
15
-
-
0141567744
-
RecQ helicases: suppressors of tumorigenesis and premature aging
-
Bachrati C.Z., and Hickson I.D. RecQ helicases: suppressors of tumorigenesis and premature aging. Biochem. J. 374 (2003) 577-606
-
(2003)
Biochem. J.
, vol.374
, pp. 577-606
-
-
Bachrati, C.Z.1
Hickson, I.D.2
-
16
-
-
30344477373
-
Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome
-
Macris M.A., Krejci L., Bussen W., Shimamoto A., and Sung P. Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome. DNA Repair (Amst.) 5 (2006) 172-180
-
(2006)
DNA Repair (Amst.)
, vol.5
, pp. 172-180
-
-
Macris, M.A.1
Krejci, L.2
Bussen, W.3
Shimamoto, A.4
Sung, P.5
-
17
-
-
30344442461
-
Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping
-
Larizza L., Magnani I., and Roversi G. Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping. Cancer Lett. 232 (2006) 107-120
-
(2006)
Cancer Lett.
, vol.232
, pp. 107-120
-
-
Larizza, L.1
Magnani, I.2
Roversi, G.3
-
18
-
-
0027493111
-
Endogenous DNA adducts: potential and paradox
-
Marnett L., and Burcham P. Endogenous DNA adducts: potential and paradox. Chem. Res. Toxicol. 6 (1993) 771-785
-
(1993)
Chem. Res. Toxicol.
, vol.6
, pp. 771-785
-
-
Marnett, L.1
Burcham, P.2
-
19
-
-
0033378084
-
Oxidative damage, bleomycin, and gamma radiation induce different types of DNA strand breaks in normal lymphocytes and thymocytes: a comet study
-
Benitez-Bribiesca L., and Sanchez-Suarez P. Oxidative damage, bleomycin, and gamma radiation induce different types of DNA strand breaks in normal lymphocytes and thymocytes: a comet study. Ann. N.Y. Acad. Sci. 887 (1999) 133-149
-
(1999)
Ann. N.Y. Acad. Sci.
, vol.887
, pp. 133-149
-
-
Benitez-Bribiesca, L.1
Sanchez-Suarez, P.2
-
20
-
-
10744225050
-
Growth retardation and skin abnormalities of the Recql4-deficient mouse
-
Hoki Y., Araki R., Fujimori A., Ohhata T., Koseki H., Fukumura R., Nakamura M., Takahashi H., Noda Y., Kito S., and Abe M. Growth retardation and skin abnormalities of the Recql4-deficient mouse. Hum. Mol. Genet. 12 (2003) 2293-2299
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2293-2299
-
-
Hoki, Y.1
Araki, R.2
Fujimori, A.3
Ohhata, T.4
Koseki, H.5
Fukumura, R.6
Nakamura, M.7
Takahashi, H.8
Noda, Y.9
Kito, S.10
Abe, M.11
-
21
-
-
0242609126
-
Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases
-
Siitonen H.A., Kopra O., Kaariainen H., Haravuori H., Winter R.M., Saamanen A.M., Peltonen L., and Kestila M. Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. Hum. Mol. Genet. 12 (2003) 2837-2844
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2837-2844
-
-
Siitonen, H.A.1
Kopra, O.2
Kaariainen, H.3
Haravuori, H.4
Winter, R.M.5
Saamanen, A.M.6
Peltonen, L.7
Kestila, M.8
-
23
-
-
0027534494
-
A case of Rothmund-Thomson syndrome with reduced DNA repair capacity
-
Shinya A., Nishigori C., Moriwaki S., Takebe H., Kubota M., and Ogino A. A case of Rothmund-Thomson syndrome with reduced DNA repair capacity. Arch. Dermatol. 129 (1993) 332-336
-
(1993)
Arch. Dermatol.
, vol.129
, pp. 332-336
-
-
Shinya, A.1
Nishigori, C.2
Moriwaki, S.3
Takebe, H.4
Kubota, M.5
Ogino, A.6
-
24
-
-
0020066137
-
Enhanced radiosensitivity and defective DNA repair in cultured fibroblasts derived from Rothmund-Thomson syndrome patients
-
Smith P.J., and Paterson M.C. Enhanced radiosensitivity and defective DNA repair in cultured fibroblasts derived from Rothmund-Thomson syndrome patients. Mutat. Res. 94 (1982) 213-218
-
(1982)
Mutat. Res.
, vol.94
, pp. 213-218
-
-
Smith, P.J.1
Paterson, M.C.2
-
25
-
-
0021984739
-
Non-dermatological complications and genetic aspects of the Rothmund-Thomson syndrome
-
Starr D.G., McClure J.P., and Connor J.M. Non-dermatological complications and genetic aspects of the Rothmund-Thomson syndrome. Clin. Genet. 27 (1985) 102-104
-
(1985)
Clin. Genet.
, vol.27
, pp. 102-104
-
-
Starr, D.G.1
McClure, J.P.2
Connor, J.M.3
-
26
-
-
0037115963
-
Oxidative nucleotide damage: consequences and prevention
-
Sekiguchi M., and Tsuzuki T. Oxidative nucleotide damage: consequences and prevention. Oncogene 21 (2002) 8895-8904
-
(2002)
Oncogene
, vol.21
, pp. 8895-8904
-
-
Sekiguchi, M.1
Tsuzuki, T.2
-
27
-
-
0035834121
-
Senescent fibroblasts promote epithelial cell growth and tumorigenesis: a link between cancer and aging
-
Krtolica A., Parrinello S., Lockett S., Desprez P.Y., and Campisi J. Senescent fibroblasts promote epithelial cell growth and tumorigenesis: a link between cancer and aging. Proc. Natl. Acad. Sci. USA 98 (2001) 12072-12077
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 12072-12077
-
-
Krtolica, A.1
Parrinello, S.2
Lockett, S.3
Desprez, P.Y.4
Campisi, J.5
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